Monofluorinated 5-membered rings via fluoromethylene transfer: synthesis of monofluorinated isoxazoline N-oxides.


Journal

Organic & biomolecular chemistry
ISSN: 1477-0539
Titre abrégé: Org Biomol Chem
Pays: England
ID NLM: 101154995

Informations de publication

Date de publication:
28 03 2021
Historique:
pubmed: 6 3 2021
medline: 6 3 2021
entrez: 5 3 2021
Statut: ppublish

Résumé

The synthesis of five-membered rings using fluoromethylene transfer chemistry is an attractive method for building fluorinated products of high value. This work demonstrates for the first time that one-fluorine-one-carbon modification of a substrate could be a viable strategy to access monofluorinated five-membered rings. The synthetic methodology was developed to access monofluorinated isoxazoline-N-oxides in one step starting from substituted 2-nitroacrylates using fluoromethylsulfonium reagents.

Identifiants

pubmed: 33666634
doi: 10.1039/d1ob00270h
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2688-2691

Auteurs

Arturs Sperga (A)

Latvian Institute of Organic Synthesis, Aizkraukles 21, LV-1006, Riga, Latvia. janis.veliks@osi.lv.

Classifications MeSH